Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort
Genet Med
.
2023 Feb;25(2):100004.
doi: 10.1016/j.gim.2022.100004.
Authors
Pleuntje J van der Sluijs
,
Marieke Joosten
,
Caroline Alby
,
Tania Attié-Bitach
,
Kelly Gilmore
,
Christele Dubourg
,
Mélanie Fradin
,
Tianyun Wang
,
Evangeline C Kurtz-Nelson
,
Kaitlyn P Ahlers
,
Peer Arts
,
Christopher P Barnett
,
Myla Ashfaq
,
Anwar Baban
,
Myrthe van den Born
,
Sarah Borrie
,
Tiffany Busa
,
Alicia Byrne
,
Miriam Carriero
,
Claudia Cesario
,
Karen Chong
,
Anna Maria Cueto-González
,
Jennifer C Dempsey
,
Karin E M Diderich
,
Dan Doherty
,
Stense Farholt
,
Erica H Gerkes
,
Svetlana Gorokhova
,
Lutgarde C P Govaerts
,
Pernille A Gregersen
,
Scott E Hickey
,
Mathilde Lefebvre
,
Francesca Mari
,
Jelena Martinovic
,
Hope Northrup
,
Melanie O'Leary
,
Kareesma Parbhoo
,
Sophie Patrier
,
Bernt Popp
,
Fernando Santos-Simarro
,
Corinna Stoltenburg
,
Christel Thauvin-Robinet
,
Elisabeth Thompson
,
Anneke T Vulto-van Silfhout
,
Farah R Zahir
,
Hamish S Scott
,
Rachel K Earl
,
Evan E Eichler
,
Neeta L Vora
,
Yael Wilnai
,
Jessica L Giordano
,
Ronald J Wapner
,
Jill A Rosenfeld
,
Monique C Haak
,
Gijs W E Santen
PMID:
36745127
PMCID:
PMC9983121
DOI:
10.1016/j.gim.2022.100004
No abstract available
Publication types
Published Erratum
Grants and funding
P50 HD103524/HD/NICHD NIH HHS/United States
R01 MH101221/MH/NIMH NIH HHS/United States